おすすめの製品
アッセイ
98%
不純物
≤2% Li2CO3
SMILES記法
[Li+].Cc1ccc(cc1)S([O-])=O
InChI
1S/C7H8O2S.Li/c1-6-2-4-7(5-3-6)10(8)9;/h2-5H,1H3,(H,8,9);/q;+1/p-1
InChI Key
MSUZXYWQEDRGFN-UHFFFAOYSA-M
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アプリケーション
Lithium p-toluenesulfinate may be used in the preparation of 2-oxo-1,3-diphenyl-1,2-dihydroquinoline-4-carbonitrile. It may be used in the preparation of highly fluorescent compound, 3-amino-6-methoxy-4-p-tolylsulfonylquinolone.
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
個人用保護具 (PPE)
Eyeshields, Gloves, type N95 (US)
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
365203-VAR:
365203-5G:
365203-BULK:
365203-25G:
Month 2013 6-Methoxy-2-oxo-1, 2-dihydroquinoline-3, 4-dicarbonitriles, A Red Compound Class with Solvent and pH Independent Green Fluorescence Maxima.
Journal of Heterocyclic Chemistry, 51, 492-501 (2014)
4-Cyano-6, 7-dimethoxycarbostyrils with Solvent-and pH-Independent High Fluorescence Quantum Yields and Emission Maxima.
European Journal of Organic Chemistry, 3, 563-571 (2008)
Journal of chromatography. A, 1129(1), 21-28 (2006-08-09)
Addition of long-chain polyunsaturated fatty acids (LC-PUFAs) from marine oil into food products implies preliminary refining procedures of the oil which thermal process affects the integrity of LC-PUFAs. Deodorization, the major step involving high temperatures, is a common process used
Journal of chromatography. A, 1214(1-2), 30-36 (2008-11-14)
In recent years, several countries have implemented new regulations regarding limitations or labeling of the trans fatty acid (tFA) content in foods. In order to comply with the new requirements, gas chromatographic methods for fatty acid (FA) analysis have been
Molecular diversity, 16(3), 591-600 (2012-08-29)
A variety of pyrazolo[3,4-d]pyrimidine-6(7H)-thione derivatives were easily synthesized with a novel, simple, efficient, and regioselective method via three-component condensation reaction of 5-methyl-1H-pyrazol-3-amine, arylisothiocyanates, and aldehydes in the presence of catalytic amount of p-toluenesulfonic acid (p-TSA) in 1-butyl-3-methylimidazolium bromide ionic liquid
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